BEUDAMED
    10 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Argos

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GELX ORAL GEL

    FDA 510(k)
    FDA Unclassified ·Unknown

    DUOCOOL PAIN MANAGEMENT PROBE, MODEL OSP-17-180-20

    FDA 510(k)
    FDA Class 2 ·Neurology

    OSSURE LOEP KIT

    FDA Adverse Event
    Death ·AGNOVOS HEALTHCARE USA, LLC·Product code MQV·December 27, 2018

    OSSURE LOEP KIT

    FDA Adverse Event
    Death ·AGNOVOS HEALTHCARE USA, LLC·Product code MQV·January 18, 2020

    EVOLUT R TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·October 16, 2018

    ENDO GIA ULTRA UNIVERSAL

    FDA Adverse Event
    COVIDIEN·Product code GDW·June 19, 2013

    ENDEAVOR RX SPRINT CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·July 21, 2011

    PULSE GEN MODEL 101

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·September 23, 2008

    EVOLUT R TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·January 2, 2019